Job Summary:

Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).

Responsibilities:

• Assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.

• Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.

• Respond to queries in a timely fashion.

• Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

• Assist multidisciplinary team in research activities.

Qualifications:

• Bachelor’s degree required or equivalent combination of education and experience.

• Medical and/or science experience/education preferred.

• Proficient with the Microsoft suite including Excel and Power point.

• Demonstrated attention to detail.

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans